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Summary Literature (1)
DOID:0111095 - Fanconi anemia complementation group A


Disease Ontology Definition:A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCA gene on chromosome 16q24.

Synonyms: FANCA,

Xenbase Genes : fancm, fanca

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009215 - Fanconi anemia complementation group A


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Fanconi anemia (is_a), autosomal recessive disease (is_a)